| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Additional considerations for CF nutritional guidelines
|
Siracusa, Christopher
|
|
|
22 |
6 |
p. 1133-1134
|
artikel
|
| 2 |
Alterations in lipids after initiation of highly effective modulators in people with cystic fibrosis
|
Despotes, Katherine A.
|
|
|
22 |
6 |
p. 1024-1026
|
artikel
|
| 3 |
A pediatric cystic fibrosis arthropathy case who responded to Elexacaftor/Tezacaftor/Ivacaftor therapy
|
Arslan, Meliksah
|
|
|
22 |
6 |
p. 1120-1122
|
artikel
|
| 4 |
Association of low-density neutrophils with lung function and disease progression in adult cystic fibrosis
|
Murru, Andréa
|
|
|
22 |
6 |
p. 1080-1084
|
artikel
|
| 5 |
Autoimmunity in people with cystic fibrosis
|
Chadwick, Christina
|
|
|
22 |
6 |
p. 969-979
|
artikel
|
| 6 |
Body mass index and nutritional intake following Elexacaftor/Tezacaftor/Ivacaftor modulator therapy in adults with cystic fibrosis
|
Caley, L.R.
|
|
|
22 |
6 |
p. 1002-1009
|
artikel
|
| 7 |
Changes in fecal elastase-1 following initiation of CFTR modulator therapy in pediatric patients with cystic fibrosis
|
Stephenson, Kimberly G.
|
|
|
22 |
6 |
p. 996-1001
|
artikel
|
| 8 |
Changes in nutrition and growth status in young children in the first 12 weeks of ivacaftor therapy
|
Tindall, Alyssa
|
|
|
22 |
6 |
p. 989-995
|
artikel
|
| 9 |
Clinical and functional efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis carrying the N1303K mutation
|
Sadras, Ido
|
|
|
22 |
6 |
p. 1062-1069
|
artikel
|
| 10 |
Clinician perspectives on barriers and solutions to symptom management in cystic fibrosis
|
Smirnova, Natalia
|
|
|
22 |
6 |
p. 1100-1103
|
artikel
|
| 11 |
Editorial Board
|
|
|
|
22 |
6 |
p. ii
|
artikel
|
| 12 |
Hidden CFSPID in CF patient registries? The Italian CF Registry experience
|
Terlizzi, V
|
|
|
22 |
6 |
p. 1128-1129
|
artikel
|
| 13 |
Human epididymis protein 4 (HE4) plasma concentration inversely correlates with the improvement of cystic fibrosis lung disease in p.Phe508del-CFTR homozygous cases treated with the CFTR modulator lumacaftor/ivacaftor combination
|
Pócsi, Marianna
|
|
|
22 |
6 |
p. 1085-1092
|
artikel
|
| 14 |
Hyperbilirubinemia and Gilbert's syndrome in Cystic Fibrosis patients treated with elexacaftor/tezacaftor/ivacaftor
|
Terlizzi, V.
|
|
|
22 |
6 |
p. 1130-1132
|
artikel
|
| 15 |
Improvement of lipid and lipoprotein profiles in children and adolescents with cystic fibrosis on CFTR modulator therapy
|
Yuzyuk, Tatiana
|
|
|
22 |
6 |
p. 1027-1035
|
artikel
|
| 16 |
Incidence of fibrosing colonopathy with pancreatic enzyme replacement therapy in patients with cystic fibrosis
|
Chiuve, Stephanie E.
|
|
|
22 |
6 |
p. 1017-1023
|
artikel
|
| 17 |
Longitudinal mental health trends in cystic fibrosis
|
Hjelm, Michelle
|
|
|
22 |
6 |
p. 1093-1099
|
artikel
|
| 18 |
Manifestation and staging of arthropathy in cystic fibrosis. Defining different stages of cystic fibrosis arthropathy using ultrasound imaging and clinical scoring
|
Holz, F.
|
|
|
22 |
6 |
p. 980-988
|
artikel
|
| 19 |
Meconium ileus and pancreatic sufficiency with D1152H mutation: A case report and review of the literature
|
Lang, Emma
|
|
|
22 |
6 |
p. 1125-1127
|
artikel
|
| 20 |
News article
|
|
|
|
22 |
6 |
p. 959-960
|
artikel
|
| 21 |
Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis children
|
Orenti, Annalisa
|
|
|
22 |
6 |
p. 1070-1079
|
artikel
|
| 22 |
Red ginseng aqueous extract improves mucociliary transport dysfunction and histopathology in CF rat airways
|
Cho, Do-Yeon
|
|
|
22 |
6 |
p. 1113-1119
|
artikel
|
| 23 |
SNSP113 (PAAG) improves mucociliary transport and lung pathology in the Scnn1b-Tg murine model of CF lung disease
|
Harris, Elex S.
|
|
|
22 |
6 |
p. 1104-1112
|
artikel
|
| 24 |
Standards for the care of people with cystic fibrosis (CF)
|
Southern, Kevin W
|
|
|
22 |
6 |
p. 961-962
|
artikel
|
| 25 |
Standards for the care of people with cystic fibrosis (CF): A timely and accurate diagnosis
|
Castellani, Carlo
|
|
|
22 |
6 |
p. 963-968
|
artikel
|
| 26 |
Successful treatment of distal intestinal obstruction syndrome with N-acetylcysteine and polyethylene glycol via colonoscopy
|
Emelogu, Ikenna K.
|
|
|
22 |
6 |
p. 1123-1124
|
artikel
|
| 27 |
The association between gut microbiome and growth in infants with cystic fibrosis
|
Deschamp, AR
|
|
|
22 |
6 |
p. 1010-1016
|
artikel
|
| 28 |
The impact of elexacaftor/tezacaftor/ivacaftor on fat-soluble vitamin levels in people with cystic fibrosis
|
Hergenroeder, Georgene E
|
|
|
22 |
6 |
p. 1048-1053
|
artikel
|
| 29 |
The natural history of cystic fibrosis liver disease a prospective cohort study
|
Rowland, Marion
|
|
|
22 |
6 |
p. 1054-1061
|
artikel
|
| 30 |
What do people with cystic fibrosis eat? Diet quality, macronutrient and micronutrient intakes (compared to recommended guidelines) in adults with cystic fibrosis–A systematic review
|
Greaney, Cian
|
|
|
22 |
6 |
p. 1036-1047
|
artikel
|
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